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CAS

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76626-01-2

benzyl-2,4,6-tribromophenylnitroxyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76626-01-2 Structure

  • Basic information

    1. Product Name: benzyl-2,4,6-tribromophenylnitroxyl
    2. Synonyms:
    3. CAS NO:76626-01-2
    4. Molecular Formula:
    5. Molecular Weight: 434.933
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76626-01-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: benzyl-2,4,6-tribromophenylnitroxyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl-2,4,6-tribromophenylnitroxyl(76626-01-2)
    11. EPA Substance Registry System: benzyl-2,4,6-tribromophenylnitroxyl(76626-01-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 76626-01-2(Hazardous Substances Data)

76626-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76626-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,2 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76626-01:
(7*7)+(6*6)+(5*6)+(4*2)+(3*6)+(2*0)+(1*1)=142
142 % 10 = 2
So 76626-01-2 is a valid CAS Registry Number.

76626-01-2Downstream Products

76626-01-2Relevant articles and documents

Initiation of radical cyclisation reactions using dimanganese decacarbonyl. A flexible approach to preparing 5-membered rings

Gilbert, Bruce C.,Kalz, Wilhelm,Lindsay, Chris I.,McGrail, P. Terry,Parsons, Andrew F.,Whittaker, David T. E.

, p. 1187 - 1194 (2000)

Photolysis of dimanganese decacarbonyl [Mn2(CO)10] using visible light produces the manganese pentacarbonyl radical [Mn(CO)5] which reacts with organohalides to form carbon-centred radicals. Efficient halogen-atom abstract

FREE RADICALS. XXII. REACTIONS OF "ELECTRON-DEFICIENT" RADICALS WITH ORGANOMAGNESIUM AND ORGANOMERCURY COMPOUNDS

Tanaseichuk, B. S.,Belozerov, A. I.,Sanaeva, E. P.,Butin, K. P.

, p. 494 - 497 (2007/10/02)

The reactions of triphenylimidazolyl and diphenylaminyl radicals with methylmagnesium iodide, phenylmagnesium bromide, and dibenzylmercury were studied.It was shown that the radicals are reduced to anions and the radicals in the organometallic compounds are displaced.The homolytic nature of the displacement of the radical from the organometallic compounds ( SH2 reaction ) is confirmed by its capture by 2,4,6-tribromonitrosobenzene with formation of a nitroxyl radical.

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